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"0093-9702-05" National Drug Code (NDC)
Carbidopa And Levodopa 500 TABLET in 1 BOTTLE (0093-9702-05)
(Teva Pharmaceuticals USA, Inc.)
NDC Code
0093-9702-05
Package Description
500 TABLET in 1 BOTTLE (0093-9702-05)
Product NDC
0093-9702
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Carbidopa And Levodopa
Non-Proprietary Name
Carbidopa And Levodopa
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20220118
Marketing Category Name
ANDA
Application Number
ANDA074260
Manufacturer
Teva Pharmaceuticals USA, Inc.
Substance Name
CARBIDOPA; LEVODOPA
Strength
25; 100
Strength Unit
mg/1; mg/1
Pharmacy Classes
Amino Acids, Aromatic [CS], Aromatic Amino Acid [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0093-9702-05